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Movement Disorders : Official Journal of the Movement Disorder Society|April 28, 2022
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An UpdateLara M Lange, Paulina Gonzalez-Latapi, Rajasumi Rajalingam, et al.
Annals of Neurology|May 19, 2026
Outcomes in Long-Term Follow-Up of Sporadic Parkinson's Disease in the Parkinson's Progression Markers InitiativePaulina Gonzalez-Latapi, Caroline Gochanour, Seung Ho Choi, et al.
Brain Communications|March 21, 2025
LRRK2-associated parkinsonism with and without in vivo evidence of alpha-synuclein aggregates: longitudinal clinical and biomarker characterizationLana M Chahine, David-Erick Lafontant, Seung Ho Choi, et al.
Medrxiv : the Preprint Server for Health Sciences|August 7, 2024
LRRK2-Associated Parkinsonism With and Without In Vivo Evidence of Alpha-Synuclein AggregatesLana M Chahine, David-Erick Lafontant, Seung Ho Choi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 28, 2026
Clinical and Imaging Characteristics of Parkinson's Disease with Negative Alpha-Synuclein Seed Amplification AssaySarah M Brooker, Jacopo Pasquini, Seung Ho Choi, et al.
NPJ Parkinson'S Disease|June 23, 2026
Primary prevention of Parkinson's disease: proceedings, the 8C's and a position statement from the Parkinson's disease prevention think tankSneha Mantri, Rhoda Au, Anastasia Barnes, et al.
The Journal of Clinical Investigation|February 4, 2021
Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystoniaNiccolò E Mencacci, Marisa M Brockmann, Jinye Dai, et al.
Trials|October 6, 2022
Study in Parkinson's disease of exercise phase 3 (SPARX3): study protocol for a randomized controlled trialCharity G Patterson, Elizabeth Joslin, Alexandra B Gil, et al.
Annals of Neurology|May 11, 2026
Expanding PPMI through Remote Data Acquisition and Analysis: Early Success and Future Growth with myPPMICaroline M Tanner, Craig E Stanley, Ethan G Brown, et al.
Annals of Neurology|August 19, 2020
Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal AbnormalitiesDora Steel, Michael Zech, Chen Zhao, et al.
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